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Journal of Medicinal Chemistry|March 11, 2009
Design, synthesis, and structure-activity relationship of substrate competitive, selective, and in vivo active triazole and thiadiazole inhibitors of the c-Jun N-terminal kinaseSurya K De, John L Stebbins, Li-Hsing Chen, et al.
Bioorganic & Medicinal Chemistry|March 14, 2009
Discovery of 2-(5-nitrothiazol-2-ylthio)benzo[d]thiazoles as novel c-Jun N-terminal kinase inhibitorsSurya K De, Li-Hsing Chen, John L Stebbins, et al.
Pigment Cell & Melanoma Research|May 20, 2011
Effective inhibition of melanoma by BI-69A11 is mediated by dual targeting of the AKT and NF-κB pathwaysYongmei Feng, Elisa Barile, Surya K De, et al.
Chemical Biology & Drug Design|May 14, 2011
Targeting metalloproteins by fragment-based lead discoverySherida Johnson, Elisa Barile, Biancamaria Farina, et al.
Oncotarget|March 10, 2016
Therapy of pancreatic cancer via an EphA2 receptor-targeted delivery of gemcitabineBridget A Quinn, Si Wang, Elisa Barile, et al.
ACS Chemical Biology|November 17, 2025
NMR and SPR Fragment-Based Screening Can Produce Novel High Affinity Small Molecule Hits against Structured RNAsBrooke X C Kwai, Indu R Chandrashekaran, Biswaranjan Mohanty, et al.
Bioorganic & Medicinal Chemistry|January 5, 2010
Synthesis and optimization of thiadiazole derivatives as a novel class of substrate competitive c-Jun N-terminal kinase inhibitorsSurya K De, Vida Chen, John L Stebbins, et al.
Pigment Cell & Melanoma Research|October 6, 2012
Inhibition of melanoma development in the Nras((Q61K)) ::Ink4a(-/-) mouse model by the small molecule BI-69A11Yongmei Feng, Eric Lau, Marzia Scortegagna, et al.
Frontiers in Oncology|June 2, 2012
An optically pure apogossypolone derivative as potent pan-active inhibitor of anti-apoptotic bcl-2 family proteinsJun Wei, John L Stebbins, Shinichi Kitada, et al.
ACS Infectious Diseases|May 19, 2015
A Potent Anti-influenza Compound Blocks Fusion through Stabilization of the Prefusion Conformation of the Hemagglutinin ProteinKris M White, Paul De Jesus, Zhong Chen, et al.
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